DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS— 510(k) K931474

Name: FDA 510(k) clearance K931474
Creator: U.S. Food and Drug Administration
Published: 1994-05-10

Unknown

Gbf Medical Group

FDA 510(k) clearance K931474 for DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS, Unknown on 1994-05-10. Applicant: Gbf Medical Group. Device class: 1.

Clearance details

Applicant: Gbf Medical Group
Product code: Code KDW
Device class: Class 1
Regulation: 21 CFR 864.3250
Advisory panel: Pathology
Date received: 1993-03-24
Decision date: 1994-05-10
Decision: Unknown
Clearance type: Traditional
Location: Greensboro, NC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KDW

view all

K970580 — SASI-DC1TS1997-04-17
K951122 — CAPITOL URINE DRUG SCREEN COLLECTION KIT1995-05-05
K913967 — DOX TAMPERPROOF SPECIMEN CONTAINER SYSTEM1991-10-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.